Canonical Allele Identifier: CA642410832
Gene: EFNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1266892308
gnomAD v2: X-68049785-G-A
gnomAD v4: X-68829942-G-A
MyVariant Identifiers: chrX:g.68049785G>A (hg19) chrX:g.68829942G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.68829942G>A , CM000685.2:g.68829942G>A GRCh38
NC_000023.10:g.68049785G>A , CM000685.1:g.68049785G>A GRCh37
NC_000023.9:g.67966510G>A NCBI36
NG_008887.1:g.5946G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000204961.5:c.128+38G>A MANE Select ENSP00000204961.4:n.128+38G>A
ENST00000204961.4:c.128+38G>A ENSP00000204961.4:n.128+38G>A
NM_004429.4:c.128+38G>A NP_004420.1:n.128+38G>A
NM_004429.5:c.128+38G>A MANE Select NP_004420.1:n.128+38G>A
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